A Novel CCT5 Missense Variant Associated with Early Onset Motor Neuropathy

Diseases associated with acquired or genetic defects in members of the chaperoning system (CS) are increasingly found and have been collectively termed chaperonopathies. Illustrative instances of genetic chaperonopathies involve the genes for chaperonins of Groups I (e.g., Heat shock protein 60, Hsp...

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Detalles Bibliográficos
Autores principales: Antona, Vincenzo, Scalia, Federica, Giorgio, Elisa, Radio, Francesca C., Brusco, Alfredo, Oliveri, Massimiliano, Corsello, Giovanni, Lo Celso, Fabrizio, Vadalà, Maria, Conway de Macario, Everly, Macario, Alberto J. L., Cappello, Francesco, Giuffrè, Mario
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7589105/
https://www.ncbi.nlm.nih.gov/pubmed/33076433
http://dx.doi.org/10.3390/ijms21207631

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7589105/
https://www.ncbi.nlm.nih.gov/pubmed/33076433
http://dx.doi.org/10.3390/ijms21207631

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